NDLClass IIImplant
Pin, Fixation, Smooth, Metallic
Orthopedic · 21 CFR 888.3040
MDR events55All time
Recalls1All time
Registered firms16Currently listed
510(k) clearances2All time
Recent MDR events
55 adverse event reports on file
- K-WIRE 0.9MM, 120MMJul 21, 2026MalfunctionTrimed, Inc.2031009-2026-00011
- UNKFeb 22, 2026MalfunctionArthrex, Inc.1220246-2026-00716
- UNKFeb 22, 2026InjuryArthrex, Inc.1220246-2026-00717
- UNKFeb 22, 2026MalfunctionArthrex, Inc.1220246-2026-00718
- UNKFeb 22, 2026InjuryArthrex, Inc.1220246-2026-00719
- UNKFeb 22, 2026InjuryArthrex, Inc.1220246-2026-00720
- UNKFeb 22, 2026InjuryArthrex, Inc.1220246-2026-00721
- UNKFeb 22, 2026InjuryArthrex, Inc.1220246-2026-00722
- UNKFeb 22, 2026InjuryArthrex, Inc.1220246-2026-00723
- UNKFeb 22, 2026InjuryArthrex, Inc.1220246-2026-00724
Event type breakdown
Injury46
Malfunction8
Other1
Recalls
1 recall events for this product code
Registered firms
16 firms currently registered for this product code
Trimed, Inc.
Santa Clarita, CA, US
Autocam Medical Devices (suzhou) Co. Ltd.
Suzhou Jiangsu, CN
Maxkron Machine, Llc
Valencia, CA, US
Apex (guangzhou) Tools & Orthopedics Company
Guangzhou Guangdong, CN
Quadm Technologies, Llc
Hamilton, NJ, US
Sterigenics Us Llc
Gurnee, IL, US
Cb Enterprises
Canyon Country, CA, US
Paragon Medical, Inc.
PIERCETON, IN, US
Sterigenics Us, Llc
Lewis Center, OH, US
Bellfx
San Fernando, CA, US
Miing Wei Co., Ltd.
Tsao-Twon Nantou, TW
510(k) clearances
2 clearances for this product code